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Home Self Checking Blood Vitamin D Rapid Test CE Approved
US$2.20
10,000-49,999 Pieces
US$2.05
50,000-99,999 Pieces
US$1.95
100,000+ Pieces
Sample price:US$0.10/piece.Request sample

Product profile

Customization

Available

Type

IVD Reagent

Certification

CE, ISO13485

Model NO.

SV-083

Classification

Ivd Reagent

Group

All Groups

Accuracy

93.8%

Sensitivity

10-30-100ng/Ml

Specimen

Fingterip Whole Blood

Format

Cassettes

Product

Vitamin D Self Testing

Quality Certification

CE, ISO13485

Usage

Pharmacy, Home Use

Transport Package

Carton

Specification

OEM

Trademark

SD

Origin

Hangzhou

HS Code

3822190090

Production Capacity

300000PCS/Day

Key features

High Accuracy: Accuracy exceeds 93.8% for reliable Vitamin D detection.
Fast Results: Read results within 5 minutes of adding buffer.
No Equipment Required: Simple operation with no special equipment needed.
CE & ISO13485 Certified: Product holds CE and ISO13485 quality certifications.
Long Shelf Life: Valid for 24 to 36 months from manufacture date.
OEM Service Available: OEM customization available with 20 days lead time.
Easy Visual Interpretation: Clear color card provided for instant result reading.
Home Use Ready: Designed for convenient self-testing at home or pharmacy.

Company profile

Business Type: Manufacturer/FactoryExport Year: 2005-08-05Nearest Port: Shanghai, TIANJINAverage Response Time: ≤9.88hTerms of Payment: T/T, PayPal, Western Union, etc.International Commercial Terms(Incoterms): FOB, EXW, CFR, CIF, DDP, DAP, FCA

AI-Powered supplier vetting

SummaryHenan Season Medical Device Co., Ltd. is identified as a Chinese manufacturer/factory specializing in point-of-care and in-vitro diagnostic self-testing products. The supplier reports eight production lines, annual Early Pregnancy HCG test output of 10,000,000 pieces, and lead times of within 15 working days in both peak and off-peak seasons. Its stated export coverage is broad, with exports accounting for 90% of total sales. ISO 9001, ISO 13485, ISO 14001, and CE/FDA-related approvals are reported. Evidence also indicates OEM packaging, R&D engineers, and quality-control staff. However, the provided information does not sufficiently establish after-sales service processes, financial credibility, or verified customer case depth. Trade data shows only one transaction, which is insufficient to demonstrate an established customer track record.
Supplier typeThe supplier is explicitly identified as a Manufacturer/Factory and Limited Company based in Zhengzhou, Henan, China. Its stated business focuses on biomedical IVD and rapid self-testing products, indicating direct manufacturing involvement rather than only trading activity.
CertificationsThe supplier reports ISO 9001, ISO 13485, and ISO 14001 certifications or approvals, and states that its products have received CE approval in Europe and FDA approval in the United States. These claims provide explicit evidence of a certification and regulatory-compliance capability, although the slices do not provide certificate numbers, validity dates, or scope details.
R&D capabilityThe supplier reports 6–10 years of R&D engineer experience and offers a broad range of rapid and self-testing products, including digital pregnancy and ovulation tests, vitamin D, UTI, syphilis, and drug tests. This supports product-development capability, although no specific patents, new-product launches, or measurable innovation outcomes are provided.
Production capacityThe supplier reports eight production lines, annual Early Pregnancy HCG test output of 10,000,000 pieces, and order fulfillment within 15 working days during both peak and off-peak seasons. Its export sales share is reported as 90%, indicating stated production and international fulfillment experience.
Customization capabilityThe supplier explicitly offers OEM packaging and states that it provides customer-specific solutions and configurations. This supports packaging-level customization, but the slices do not confirm broader customization such as formulation, tooling, labeling compliance, or product design changes.

Product Q&A

Q:How does the Vitamin D test work?
A:
In medicine, a 25-hydroxy Vitamin D is the main storage form of vitamin D in the body. Therefore, the overall status of vitamin D can be determined by detecting the content of 25-hydroxy Vitamin D. 25-hydroxy Vitamin D level less than 30 ng/mL in case of a positive result, indicates Vitamin D Deficiency or Insufficiency. Vitamin D supplements can be recommended in these cases.
Q:When should the test be used?
A:
The clinical application of 25-hydroxy Vitamin D is mainly for diagnosis, treatment and monitoring of rickets (children), osteomalacia, postmenopausal osteoporosis and renal osteopathy. Vitamin D deficiency is also associated with many other diseases, including cancer, cardiovascular disease, autoimmune diseases, diabetes and depression. Monitor your vitamin D levels to determine whether to take vitamin D supplements. The Vitamin D Rapid Test can be used any time of the day.
Q:Can the result be incorrect?
A:
The results are accurate as far as the instructions are carefully respected. Nevertheless, the result can be incorrect if the Vitamin D Rapid Test cassette gets wet before test performing or if the quantity of blood dispensed in the sample well is not sufficient, or if the number of buffer drops are less than 2 or more than 3. The capillary dropper provided in the box allows making sure the collected blood volume is correct. Besides, due to immunological principles involved, there exist the chan
Q:How to interpret the test if the color and the intensity of the lines are different?
A:
Please refer to the illustration and compare the T line intensity with 'Vitamin D Color card' provided with the kit.
Q:If I read the result after 20 minutes, will the result be reliable?
A:
No. The result should be read at 10 minutes after adding the buffer. The result is unreliable after 20 minutes.

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